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TargetHistone deacetylase 4 [653-1084,H976Y]
LigandBDBM25146
Substrate/CompetitorBDBM25143
Meas. Tech.HDAC Activity Assay
Temperature298.15±n/a K
IC50 6000±n/a nM
Commentsextracted
Citation Jones, PAltamura, SDe Francesco, RPaz, OGKinzel, OMesiti, GMonteagudo, EPescatore, GRowley, MVerdirame, MSteinkühler, C A novel series of potent and selective ketone histone deacetylase inhibitors with antitumor activity in vivo. J Med Chem51:2350-3 (2008) [PubMed]  Article
More Info.:Get all data from this article,   Solution Info,  Assay Method
 
Histone deacetylase 4 [653-1084,H976Y]
Name:Histone deacetylase 4 [653-1084,H976Y]
Synonyms:HDAC4 | HDAC4_HUMAN | Histone Deacetylase 4 (HDAC4) Mutant (H976Y) | Histone deacetylase 4 gain of function (GOF) mutant | KIAA0288
Type:Catalytic domain
Mol. Mass.:46476.72
Organism:Homo sapiens (Human)
Description:His-tagged HDAC4 GOF(gain of function, H976Y) catalytic domains (T653-L1084) was expressed in E.coli and purified by Nickel-Chelation affinity chromatography and anion exchange (MonoQ) chromatography.
Residue:432
Sequence:
TTGLVYDTLMLKHQCTCGSSSSHPEHAGRIQSIWSRLQETGLRGKCECIRGRKATLEELQ
TVHSEAHTLLYGTNPLNRQKLDSKKLLGSLASVFVRLPCGGVGVDSDTIWNEVHSAGAAR
LAVGCVVELVFKVATGELKNGFAVVRPPGHHAEESTPMGFCYFNSVAVAAKLLQQRLSVS
KILIVDWDVHHGNGTQQAFYSDPSVLYMSLHRYDDGNFFPGSGAPDEVGTGPGVGFNVNM
AFTGGLDPPMGDAEYLAAFRTVVMPIASEFAPDVVLVSSGFDAVEGHPTPLGGYNLSARC
FGYLTKQLMGLAGGRIVLALEGGYDLTAICDASEACVSALLGNELDPLPEKVLQQRPNAN
AVRSMEKVMEIHSKYWRCLQRTTSTAGRSLIEAQTCENEEAETVTAMASLSVGVKPAEKR
PDEEPMEEEPPL
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  Blast E-value cutoff:
BDBM25146
BDBM25143
NameBDBM25146
Synonyms:2-(5-methoxy-2-methyl-1H-indol-3-yl)-N-[(1S)-7-oxo-1-(5-phenyl-1H-imidazol-2-yl)octyl]acetamide | 4-phenylimidazole, 17 | CHEMBL407959
TypeSmall organic molecule
Emp. Form.C29H34N4O3
Mol. Mass.486.6053
SMILESCOc1ccc2[nH]c(C)c(CC(=O)N[C@@H](CCCCCC(C)=O)c3nc(c[nH]3)-c3ccccc3)c2c1 |r|
Structure
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